A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6566011



Internal ID20939082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:86163541..86182242hg38UCSC Ensembl
chr6:86873259..86891960hg19UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg3818702
hg1918702
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18274839
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6566011
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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